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3-Cyclopentene-1-Carboxylic Acid Ethyl Ester

    • Product Name 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester
    • Alias Ethyl 3-cyclopentene-1-carboxylate
    • Einecs 212-314-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    VTB
    Specifications

    HS Code

    635918

    Chemical Name 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester
    Molecular Formula C8H12O2
    Molecular Weight 140.18 g/mol
    Cas Number 25594-19-0
    Appearance Colorless to pale yellow liquid
    Boiling Point 191-193°C
    Density 1.02 g/cm³
    Refractive Index 1.456-1.458
    Flash Point 73°C
    Solubility Insoluble in water; soluble in most organic solvents
    Smiles CCOC(=O)C1CCC=C1
    Inchi InChI=1S/C8H12O2/c1-2-10-8(9)7-5-3-4-6-7/h3,5H,2,4,6H2,1H3

    As an accredited 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 100 mL clear glass bottle, tightly sealed with a screw cap, labeled with product, hazard, and handling information.
    Shipping 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is typically classified as a non-hazardous liquid, but should be handled with care and shipped according to local regulations. Use appropriate labeling and compliant packaging to prevent leaks during transit.
    Storage Store **3-Cyclopentene-1-Carboxylic Acid Ethyl Ester** in a cool, dry, well-ventilated area away from heat, sparks, and open flames. Keep container tightly closed and protected from light and moisture. Avoid storing with oxidizing agents or strong acids. Use only with appropriate chemical safety containment (e.g., flammable liquids cabinet), and label containers clearly to prevent misuse or accidental mixing.
    Application of 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester

    Applications of 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester in Industrial Manufacturing

    3-Cyclopentene-1-Carboxylic Acid Ethyl Ester is a highly specialized cyclopentene derivative used as a building block in several chemical synthesis routes. As a direct manufacturer, we supply this raw material into advanced downstream production chains, where it plays a critical role in either structural, functional, or active ingredient development. Below are the main industrial applications, including regulatory compliance, recommended dosage, process integration, and typical finished goods.

    1. Active Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers use this material as a core intermediate in the synthesis of cyclopentene-based drug candidates and complex APIs. It enables the formation of key carbon frameworks, especially in non-aromatic ring systems required for new pharmaceutical entities. The compound supports stereospecific transformations in hydrogenations, amidations, and selective hydrolysis steps present in modern drug development schemas.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP/NF and EP monographs for in-process control (as relevant to API synthesis)
    • 21 CFR Part 210/211 (US FDA GMPs for pharmaceuticals)
    • EDQM CEP requirements for European supply chains

    Typical usage ratio

    • Usage rates range from 2% to 12% mol/mol relative to the main API target, adjusted for route optimization and molar efficiency in multistep synthesis.

    Downstream process integration

    • Integrated in early to mid-stage synthesis as a starting material for ring-forming reactions, often via Grignard addition, hydrolysis, or amide coupling steps. Subsequent derivatizations depend on target molecule backbone complexity.

    Final product types

    • Investigational and commercial APIs containing cyclopentane or cyclopentene moieties
    • Advanced pharmaceutical intermediates (APIs-in-progress)
    • Small molecule drug candidates for CNS, cardiovascular, and antiviral therapies
    • Peptidomimetic backbone intermediates

    2. Agrochemical Synthesis (Herbicide and Insecticide Building Block)

    Major agrochemical producers incorporate 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester into multistep synthesis of selective herbicide and insecticide actives, particularly those utilizing cyclopentene motifs for improved activity and environmental persistence. The ester functionality is valued for smooth conversion via transesterification or hydrolysis into acid intermediates, which then undergo further modifications.

    Industry compliance standards

    • FAO/WHO Technical Guidelines for Pesticide Specification and Quality
    • REACH Registration for intermediate use in the EU
    • OECD Principles of Good Laboratory Practice (GLP) for nonclinical testing
    • ISO 9001:2015 for Quality Management Systems in chemical manufacturing

    Typical usage ratio

    • Concentration between 5% and 20% w/w in custom synthesis steps, with precise ratio determined by process route and molecular target complexity.

    Downstream process integration

    • Enters at initial or intermediate synthesis stages, mainly via base-catalyzed condensation, followed by functional group transformations. Often precedes cyclization or halogenation in active compound assembly.

    Final product types

    • Selective herbicide AIs (e.g., cyclopentene-based post-emergence controls)
    • Novel insecticide actives with cyclopentene scaffolds
    • Agrochemical test compounds for R&D pipelines
    • Protected intermediates for patent-submitted formulations

    3. Fragrance and Flavor Intermediate Production

    In the specialty chemicals sector, manufacturers utilize this molecule for producing cyclopentene-derived building blocks used in fragrance aldehydes, musk analogues, and certain flavor ingredients. The ethyl ester group facilitates downstream selective reduction and cyclization needed to tailor scent and taste characteristics for consumer applications.

    Industry compliance standards

    • IFRA Code of Practice for fragrance compound usage
    • Food Chemical Codex (FCC) where food flavor intermediates are utilized
    • ISO 22716:2007 for cosmetic industry Good Manufacturing Practices
    • EU Regulation (EC) No 1223/2009 (Cosmetics Regulation)

    Typical usage ratio

    • In intermediate synthesis, concentrations typically range from 3% to 15% by weight of batch material for further derivatization or blending, adjusted for desired end-note complexity.

    Downstream process integration

    • Deployed during early-stage synthesis for ring introduction, then carried through hydrogenation, acylation, or cyclization steps to generate aldehyde or ester mix-ins that serve as fragrance or flavor precursors.

    Final product types

    • Fragrance aldehyde building blocks for fine chemicals
    • Cyclopentene-based musks for personal care fragrances
    • Flavor compound intermediates for beverage and confectionery formulations
    • Signature aroma chemicals for perfumery and home care

    4. Specialty Polymer Synthesis (Cyclopentene-Based Polymeric Materials)

    R&D and small-batch polymer houses use this ester to introduce cyclic moieties into polymer backbones or side chains, modifying glass transition temperature and mechanical flexibility. It enables fine-tuning of optical and resilience properties in specialty coatings, adhesives, and resin systems, especially where certain cyclic ring content is required for end-use performance.

    Industry compliance standards

    • ISO 9001:2015 for quality systems in polymer processing
    • ASTM D256, D638, D790 for polymer mechanical testing methods
    • EU Regulation (EC) No 1907/2006 (REACH) for polymers in Europe
    • RoHS compliance for electronics and coated finished goods

    Typical usage ratio

    • Ranges from 0.5% to 8% by monomer weight, controlled according to desired ring content, crosslink density, and target molecular weight of the final polymer or copolymer.

    Downstream process integration

    • Added during pre-polymerization or as a comonomer in free-radical or step-growth polymerizations. Subsequent curing or extrusion integrates the cyclic ester into the network structure, supporting enhanced durability or modulus.

    Final product types

    • Modified resins for optical coatings and adhesives
    • Block copolymers for elastomeric applications
    • Cyclopentene-rich specialty plastics for research and electronics
    • Performance composites for industrial components

    5. Fine Chemical and Analytical Reference Material

    Chemical analysts and research organizations procure this compound as a highly pure reference standard or fine chemical for method validation and impurity profiling. The molecule’s well-defined structure enables development and calibration of quantitative analysis tools in pharmaceutical and agrochemical QC labs, ensuring traceability of intermediates in regulatory submissions.

    Industry compliance standards

    • ISO 17034:2016 for reference material producers
    • USP and EP guidelines for analytical reference standards
    • GLP (OECD Guidelines) for analytical validation
    • ISO/IEC 17025 for chemical testing laboratories

    Typical usage ratio

    • Used in microgram to low milligram quantities for calibration, spiking, and development runs; quantity is dictated by detection limits and analytical technique sensitivity.

    Downstream process integration

    • Deployed in HPLC, GC, NMR, and MS method calibration cycles; used for system suitability tests, impurity identification, or stability studies in pharmaceutical and agrochemical pipelines.

    Final product types

    • Certified reference standards for internal QC or regulatory submissions
    • Impurity markers for pharmaceutical and agrochemical process control
    • Validation batches for analytical method development labs
    • Spiking solutions for recovery studies in regulated environments
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    Certification & Compliance
    More Introduction

    3-Cyclopentene-1-Carboxylic Acid Ethyl Ester: Experience from the Factory Floor

    Introduction

    We produce 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester day after day, not because it's a trendy molecule, but because our partners in pharmaceuticals, agrochemicals, and flavors need a building block they can trust. This ester—sometimes recognized by the shorthand CPCE—offers a unique blend of reactivity and stability, shaped first by the cyclopentene core and again by the ethyl ester functional group. Decades of working with cyclic intermediates have taught us the subtle differences one structural tweak can bring to an entire batch, and those lessons find their way into every drum and bottle we dispatch.

    Model and Specifications

    Looking at the compound, its structure is straightforward: a cyclopentene ring with a carboxylic acid esterified to an ethyl group. You’ll find the substance as a clear colorless liquid, carrying a faint, sometimes sweet odor thanks to the ester. The molecular weight clocks in at 140.18 g/mol. Purity by area percentage via GC regularly exceeds 98%, confirmed by our QC on every production lot. Moisture content runs below 0.5%—we use anhydrous conditions from start to finish, because trace water can trigger side reactions or hydrolysis, affecting everything from shelf life to downstream yield.

    As for physical handling, the ester boils off around 78-80°C under reduced pressure. In open systems, expect volatility to increase, so we recommend processing with proper ventilation. Density sits near 1.01 g/cm³ at 20°C. Our storage guidelines come from hard experience: stainless steel or glass containers in a cool, inert atmosphere. Ignore those steps and you’ll risk polymerization, especially if you leave it exposed to heat or light.

    Production Process Insights

    Making this ester in commercial volumes takes more than just glassware and good intentions. The heart of our process is a cyclopentene ring-opening-then-closure reaction, followed by direct esterification with high-purity ethanol. We lean on a proprietary acid catalyst blend—years ago, we swapped out traditional sulfuric for something less prone to causing side-products and corrosion, and we haven’t looked back. Because we don’t batch in glass reactors for fun, but to keep metal ions from promoting unwanted rearrangements that can slip past a casual check.

    Our raw materials matter. Poor cyclopentenes carry over sulfur, halogens, or simple dirt that end up as non-volatile residues, increasing purification hassles. Getting the water content right sounds simple but takes care—misjudgment leads to hydrolysis of the ester or, worse, polymerization in the pot. That’s especially true scaling from lab to multi-ton scale: azeotropes, vacuum levels, and separator efficiency all play critical roles in yield and purity. Recovery loops for ethanol and side-product removal don’t just keep environmental controls tight; they keep our process costs in line, and that value passes directly to formulators.

    Why Customers Rely on This Molecule

    The main value of 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester comes from its dual character. The cyclopentene olefin offers a reactive double bond, while the ester manages to stay stable enough for a host of downstream transformations. Specifying this molecule lets synthetic chemists build in exactly the right reactivity step, limiting the need for harsh reagents later in the sequence. In medicine, the backbone feeds into key intermediates for antiviral, anti-inflammatory, or cardiovascular projects. Chemists aiming for targeted biological activity appreciate predictability and batch consistency, both of which result from a robust, watched-over production line.

    In the agrochemical world, we’ve watched customers build selective herbicides and insect attractants where specificity starts with picking the right starting material. The activity or inactivity of a molecule in soil, sun, or living systems can hang on a subtle difference in ring structure or ester group. Using a consistent, high-quality CPCE, researchers can focus on designing new actives without losing time debugging impurities, tars, or shifts in boiling points.

    Flavor and fragrance firms exploit the compound’s mild volatility and reactivity to create cyclic esters or ketones with sensory profiles unattainable from cheaper ketones or open-chain esters. Because we stick to strict purification, only trace by-products linger—minimizing off-odors or color changes as the product ages on warehouse shelves.

    Differences from Other Building Blocks

    There’s no shortage of carboxylic esters with cyclic rings. What sets 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester apart is the balance of reactivity and shelf stability. Cyclopentanecarboxylic acid ethyl ester often feels more inert, but it misses the double bond that makes CPCE such a versatile synthon for ring-opening, dimerization, or simple Michael reactions. Go with open-chain analogs—like ethyl butenoate—and you lose the ability to exploit ring strain and olefin chemistry, critical for certain polymerization and functionalization strategies.

    We’ve seen customers try methyl instead of ethyl esters, or swap in saturated rings. While methyl esters sometimes work, the extra volatility increases hazards and complicates storage. Some customers tempted by cyclohexene-based esters often circle back to CPCE, realizing that size, unsaturation, and hydrophobicity interact in hard-to-predict ways during later stages. We keep getting feedback that for cyclization, Diels-Alder, and enolate chemistry, this material outperforms other candidates, saving both time and headaches in scale-up.

    We’ve found the differences between this ester and alternatives go beyond reactivity. During purification and formulation, CPCE interacts predictably with common solvents such as dichloromethane, acetonitrile, and toluene. Downstream partners appreciate that they rarely face solubility surprises or need to trial endless array of cosolvents. Most users in bench shops and factories alike can merge our ester into their process flows without costly process revalidation. Every step we take upstream—stringent drying, exclusion of oxidation-prone species, and clean distillation—pays off on their end in the form of fewer failed reactions and higher downstream yields.

    Meeting Client Expectations: Our Experience

    Clients notice the difference between trader-sourced and manufacturer-driven compounds. We control every aspect, from vetting starting materials through daily batch monitoring in in-house QC labs. Instead of relying solely on a certificate of analysis, our clients count on detailed batch records and impurity profiles, updated with every delivery. Development chemists have invited our team to inspect their lines occasionally, and each time we pick up small improvements—whether it’s a shipping tweak or an impurity control trick—that make our production even more dialed in.

    Because we handle the entire process, we fix problems directly. If a yield shift shows up in a customer’s run, we don’t pan off questions to a middleman. Rather, we jump back to our handled samples and logs, then offer troubleshooting based on actual plant data—be that aging studies, chromatogram sharing, or fresh samples pulled from the same mother lot. The real backbone of quality is responding in real-time, guided by experience, not just protocol checklists.

    Typical Applications—What Works and What Doesn’t

    Over the years, CPCE has fueled research and production for everything from active pharmaceutical intermediates to novel materials. In drug discovery, its ability to take part in regioselective transformations has led to a small but growing number of trial-stage APIs. One medicinal synthesis group turned to us after finding that commercial cyclopentenes with variable purity had derailed a multistep program. Their endpoint titer increased by 15% after switching to a reliable supply, costs fell, and batch failure rates dropped dramatically.

    In the world of crop science, several protocols make use of the ester for quick ring-opening reactions that feed into lactone synthesis. The cyclopentene double bond opens an easy route to more functionalized five-membered rings not easily available from linear precursors. Boats of intermediates built on this backbone help create more selective, eco-friendly herbicides for crops ranging from wheat to soybeans.

    Some clients see value using CPCE in flavor chemistry, particularly those blending cyclic esters for tobacco and beverage aromas. The mild, fresh note it brings out in certain profiles arises partly from its relatively low odor threshold and chemical stability under standard blending conditions. In our experience, off-odor complaints have nearly vanished since we tuned our purification regimen—it’s a point of pride that our lot tracking system can associate sensory results directly with specific operating conditions and feedstocks.

    Potential Challenges and Solutions from a Manufacturer’s Viewpoint

    Producing high-purity esters like CPCE throws unique challenges. Trace acid or base leads to runaway reactions or product degradation. Carbonyl impurities sneak in via oxidized solvents or rusty transfer lines, so we intervene directly on the production line by flushing and passivating metal hardware. Customers who require material for regulated pharmaceutical use ask for impurity profiles, especially for aldehydes and volatile carbonyls. Our in-process monitoring ensures each lot passes the tightest limits—if a parameter ever creeps out of spec, the batch doesn’t ship. Full stop.

    A recurring challenge: controlling water content. Even the slightest misbalance between drying stage and collection tanks leads to hydrolysis. Our plant operators track Karl Fischer titrations before the product leaves the reactor. Any batch off-spec is held, retreated, and requalified before shipment. This attention to hydration means our material hits target specifications consistently, not just at the start or end of a campaign, but every single container.

    Customers sometimes ask about scaling to higher volumes or adjusting concentration for greater process efficiency. Our response is based on data, not just capacity claims. We regularly map pilot trials to full-scale production, adjusting parameters—such as agitation and vapor phase zone design—to keep product quality and yield tightly controlled. Insights from these efforts help clients avoid surprises that come from simple tank-filling or from faint regional differences in local ethanol sources and water content.

    Another hurdle lies in logistics. The ester remains stable as long as it stays sealed and kept away from strong light or oxidizing agents. We’ve had a case where a summer shipment in hot, humid weather reached a client with minor polymerization. It prompted us to overhaul our packaging and ethical shipping practices: now, each container uses high-barrier linings, and our shipping policies stress controlled temperature routes whenever possible.

    Our in-house technical team supports client trials directly, helping adapt their purification or synthesis schemes to real-world plant conditions. Sometimes that means spending early mornings on the phone with a user sifting through liquid-liquid extraction challenges, or finding a workaround for an unexpected emulsion during scale-up. Direct contact means our feedback loop stays fast and useful; customers get more than just material, they get troubleshooting and practical insight drawn from years of running the same chemistry.

    Looking Ahead: Future Development and Responsible Practices

    We recognize that supply chain transparency matters. Every batch’s journey can be tracked from received raw material through to finished product, down to the solvent lots and cleaning records. Sustainability isn’t a slogan here, it’s a daily target. By integrating solvent recovery, closed handling systems, and accurate waste tracking, our facility has cut both resource use and environmental impact. These steps may take more investment and staff training, but they reduce operational risk and assure customers of supply even when global prices spike or feedstocks tighten.

    Quality doesn’t stop at our gate. We share data on residual solvents and heavy metals—wherever possible, we beat ICH and local pharmacopeia limits. Each improvement, be it a better catalyst or process control tweak, filters into our consistency and makes our material more attractive to compliance-focused clients. Whenever possible, we solicit downstream feedback, so real-world use shapes production policies. Regulatory trends—REACH, TSCA, or local—receive continuous monitoring, and any changes prompt fast adaptation in our paperwork and processes.

    We do more than just react to the market. Years producing CPCE have taught us where the demanding end-uses are growing. Contract partners look for smaller minimum orders for R&D, large drums for production, or just-in-time shipments to avoid waste. Fulfilling these needs draws on our logistic flexibility, whether dividing lots for specialty users or scaling high-throughput capacity for steady campaign production.

    Running a chemical factory is more than technical equipment; it’s experience, troubleshooting, and attention to every step. Customers that rely on 3-Cyclopentene-1-Carboxylic Acid Ethyl Ester for their own production lines see the difference that commitment makes. From precise specifications to direct technical support and robust logistics, we keep working at every detail so their chemistries stay dependable and successful.